Status:

NOT_YET_RECRUITING

A Study to Assess the Relative Bioavailability of Different Subcutaneous Formulations ofAZD6234

Lead Sponsor:

AstraZeneca

Collaborating Sponsors:

Quotient Sciences

Conditions:

Healthy Participants

Eligibility:

All Genders

18-55 years

Phase:

PHASE1

Brief Summary

This study in healthy volunteers aims to compare blood levels and side effects after administration of different formulations of AZD6234. This study will take place at one site in Nottingham, United ...

Detailed Description

This study in healthy volunteers aims to compare blood levels and side effects after administration of different formulations of AZD6234. This study will take place at one site in Nottingham, United ...

Eligibility Criteria

Inclusion

  • Healthy males or non-pregnant, non-lactating females aged 18 to 55 years inclusive
  • BMI of 25.0 to 35.0 kg/m2 inclusive and weight ≥50 kg

Exclusion

  • History of any clinically important disease or disorder
  • History or presence of clinically significant cardiovascular, renal, hepatic, dermatological, respiratory, neurological, psychiatric or gastrointestinal disorder including a history of pancreatitis or gall stones
  • Any clinically significant illness, medical/surgical procedure, or trauma within 4 weeks of the planned first dosing day
  • Clinically significant abnormal clinical chemistry, haematology, coagulation or urinalysis
  • Any clinically significant abnormal findings in vital signs
  • Any clinically significant abnormalities on 12-lead ECG
  • HbA1c ≥6.5% (≥48 mmol/mol)
  • Evidence of renal impairment
  • Females who are pregnant or lactating.
  • Any participant who has received an amylin analogue containing preparation within the last 30 days or 5 half-lives of the drug (whichever is longer)
  • Participants who report to have previously received AZD6234.
  • Use of any prescribed or non-prescribed medication

Key Trial Info

Start Date :

November 10 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

March 24 2026

Estimated Enrollment :

21 Patients enrolled

Trial Details

Trial ID

NCT07220954

Start Date

November 10 2025

End Date

March 24 2026

Last Update

October 24 2025

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Research Site

Ruddington, United Kingdom, NG11 6JS